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Reporte zur Charge U7055BA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CO 3 AL 2 WA 1 OR 1 NC 1 AK 1 CA 1 TX 1

VAERS 2288080

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

schwer
Staat
WA
Alter
12,0
Geschlecht
F
Eingang
20.05.2022
Impfdatum
20.05.2022
Beginn
20.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Seizure

Symptomtext

Patient received Tdap (Adacel) vaccine in consultation in the pharmacy with mother in the room. Patient began what appeared to be convulsing with a duration of less than one minute. Patient did not exhibit any additional symptoms after initial presentation. Emergency services were contacted per her mother's request, and patient and mother left the store with them.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
Amoxicillin
Vorherige Impfungen
-

VAERS 2206382

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

schwer
Staat
-
Alter
87,0
Geschlecht
M
Eingang
04.02.2022
Impfdatum
09.11.2021
Beginn
29.11.2021
Tage bis Beginn
20,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Guillain-Barre syndrome

Symptomtext

Narrative: 86 year-old male received Tdap booster shot on 11/9 at clinic. After the shot, he reported he was admitted to Medical Center for a week due to Guillain-Barre syndrome. After discharge from Medical Center, he was in Rehab Center. He was released on 11/27. No documented information information recorded about his hospital stay in Medical Center or Rehab.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2119274

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

mild
Staat
AL
Alter
60,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
17.02.2022
Beginn
17.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bite Inappropriate schedule of product administration Pain in extremity

Symptomtext

Patient came in to receive a tetanus shot after having a bite incident at work today. She knew that her last tetanus vaccine was in 2011. The vaccine was administered and the patient said that her arm was just sore. The patient asked for a printout of her vaccination history and it was noticed that she received an adacel vaccine on 01/14/2022. The manufacturer was contacted. He said the most common reaction for receiving a vaccine out of series and so close to the last administered date was a hypersensitivity reaction and a sore arm. He said that the patient needed to monitor for those reactions. The patient was contacted via phone and she said that she didn't have any current symptoms of a reactions other than the sore arm that she mentioned after she received the vaccine. The patient said that she would monitor for any reaction.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Tramadol, methadone, and lortab
Vorherige Impfungen
-

VAERS 2073091

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

mild
Staat
-
Alter
65,0
Geschlecht
F
Eingang
28.01.2022
Impfdatum
26.01.2022
Beginn
27.01.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Headache Injection site cellulitis Pain in extremity Pyrexia

Symptomtext

24 hours after administration of administration of TDAP and pneumovax, patient developed fever, headache, and right arm pain. Seen 1/28 and diagnosed with cellulitis to right arm at administration site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
No tests ran, clinical diagnosis
Aktuelle Erkrankungen
-
Vorgeschichte
Chronic Small Cell Lymphoma Hypothyroid
Andere Medikamente
Levothyroxine
Allergien
-
Vorherige Impfungen
-

VAERS 2039490

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

mild
Staat
OR
Alter
75,0
Geschlecht
M
Eingang
17.01.2022
Impfdatum
08.01.2022
Beginn
16.01.2022
Tage bis Beginn
8,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pruritus Rash erythematous Rash pruritic Vaccination site rash

Symptomtext

Rash on vaccination site on deltoid. Started as itchy, raised rash covering left upper arm. From picture from yesterday, my impression papular rash. Picture from today, showed rash changed to smooth surface today but still with redness. Patient denied pain but says area increased. Patient contacted pcp and waiting for call back. He did not appear in distress. I advised to watch and wait since it appeared to have improved. I advised to seek further treatment if rash symptoms worsen or if becomes painful.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ATORVASTATIN
Allergien
NON
Vorherige Impfungen
-

VAERS 1908664

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

mild
Staat
NC
Alter
-
Geschlecht
F
Eingang
30.11.2021
Impfdatum
15.11.2021
Beginn
15.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy Hypersensitivity Injection site erythema Injection site inflammation Injection site nodule Injection site swelling Injection site warmth

Symptomtext

allergic reaction to that arm; small knot around the injection site and that this morning it was a little worse; it is pink and the size of a base ball; that it is pink and the size of a base ball. She states that it is "warm to the touch and swollen but not hard but she has got some swelling there; warm to the touch; swollen but not hard but she has got some swelling there; a pregnant patient received a Tdap vaccine (it was confirmed to be Adacel); Initial information received on 17-Nov-2021 regarding an unsolicited valid non-serious case from a other health professional via the Agency (under the reference 00862766). This case involves a 34 year-old female patient who experienced allergic reaction to that arm (hypersensitivity), small knot around the injection site and that this morning it was a little worse (vaccination site nodule), it is pink and the size of a base ball (vaccination site erythema), warm to the touch (vaccination site warmth), swollen but not hard but she has got some swelling there (vaccination site swelling) and (vaccination site inflammation) after receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] (exposure during pregnancy). Data regarding this pregnancy were received prospective. The date of last menstrual period was not reported. The estimated due date was not reported. The patient past medical history, medical treatment, vaccination and family history were not provided. The patient had unknown previous pregnancy. On 15-Nov-2021, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U7055BA and expiry date: 03-Jun-2023) (Frequency once) via intramuscular route in the right deltoid for prophylactic vaccination. On an unknown date, the patient developed a non-serious allergic reaction to that arm (hypersensitivity), small knot around the injection site and that this morning it was a little worse (vaccination site nodule), pink and the size of a base ball (vaccination site erythema), warm to the touch (vaccination site warmth) and swollen but not hard but she has got some swelling there (vaccination site swelling) (vaccination site inflammation) (unknown latency) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. It was also the case of vaccine exposure during pregnancy (latency same day). It was reported "The nurse states that on Monday a pregnant patient received a Tdap vaccine (it was confirmed to be Adacel) and the patient came back to the office today with an "allergic reaction to that arm". The nurse would like to know if she can provide the AE information verbally or if she has to fill out a form. The patient was coming back today for another unrelated appointment. The nurse states that it is pink and the size of a base ball. She states that it is "warm to the touch and swollen but not hard but she has got some swelling there". Details of laboratory data not reported. The patient was treated with BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE] and advised ice and either Benadryl cream or capsules. At time of reporting, the outcome of the event was unknown for all events. Additionally, at time of reporting, the outcome of the pregnancy is unknown. There will be no information available on the batch number for this case.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1795575

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

mild
Staat
AK
Alter
11,0
Geschlecht
M
Eingang
18.10.2021
Impfdatum
13.10.2021
Beginn
14.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site swelling Injection site warmth

Symptomtext

RAISED, RED REACTION AT INJECTION SITE. it was red and warm to the touch

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
MULTIVITAMIN
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2168118

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge U7055BA

gering
Staat
CA
Alter
22,0
Geschlecht
F
Eingang
09.03.2022
Impfdatum
08.03.2022
Beginn
08.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

Pt received 2 doses of tdap. 1 in 08/30/21 and a second on 03/08/22. No adverse reaction noted on the second dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
NA
Allergien
None
Vorherige Impfungen
-

VAERS 2147459

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

gering
Staat
AL
Alter
60,0
Geschlecht
F
Eingang
27.02.2022
Impfdatum
14.01.2022
Beginn
17.02.2022
Tage bis Beginn
34,0
Dosis
2
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

an extra dose of ADACEL was administered to a patient with no ae; Initial information received on 17-Feb-2022 regarding an unsolicited valid non-serious case received from a physician. This case involves a 60 years old female patient who experienced an extra dose of adacel was administered to a patient with no ae while receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 14-Jan-2022, the patient received a first dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot U7055BA,ED : 03-06-2023 via intramuscular route with left deltoid administration site. On 17-Feb-2022 she also received a second dose of the same vaccine lot U7055BA,ED : 03-06-2023 via intramuscular route with left deltoid administration site and patient developed a non-serious event "an extra dose of adacel was administered to a patient with no adverse event" (extra dose administered) 1 month 3 days following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken with DIPHTHERIA, TETANUS AND ACELLULAR PERTUSSIS VACCINE (ADACEL) was not applicable. It was not reported if the patient received a corrective treatment for the event (an extra dose of ADACEL was administered to a patient with no ae). At time of reporting, the outcome was Unknown for the event an extra dose of adacel was administered to a patient with no ae. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1923103

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

gering
Staat
CO
Alter
-
Geschlecht
U
Eingang
04.12.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

vaccine were exposed to negative 7.7 degree celsius for 30 days /no AE; Initial information received on 18-Nov-2021 regarding an unsolicited valid non-serious case received from a other health professional and non health care professional via Medical Information (MI) number: 00864804. This case involves an unknown age and unknown gender patient who was administered INFLUENZA QUADRIVALENT RECOMBINANT VACCINE [FLUBLOK QIV], DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC], DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE [FLUZONE HD] (product storage error). The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE lot number: UJ702AC and expiry date: 30-JUN-2022 via unknown route in unknown administration site, a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot number: U7055BA and expiry date: 03-JUN-2023 via unknown route in unknown administration site, a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE lot number: C5774BA and expiry date: 18-SEP-2022 via unknown route in unknown administration site, a dose of suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT lot number: U6831AA and expiry date: 08-OCT-2022 via unknown route in unknown administration site and a dose of suspect INFLUENZA QUADRIVALENT RECOMBINANT VACCINE lot number: QFAA2110 and expiry date: 01-JUN-2022 via unknown route in unknown administration site for prophylactic vaccination respectively. It was case of an actual medication error due to Product storage error temperature too low (latency: same day). At the time of reporting, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1921704

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

gering
Staat
TX
Alter
42,0
Geschlecht
F
Eingang
03.12.2021
Impfdatum
05.11.2021
Beginn
22.11.2021
Tage bis Beginn
17,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Skin warm Swelling

Symptomtext

REDNESS, SWELLING WARM TO TOUCH ADVIL AND BENADRYL CREAM

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ADVIL AND BENADRYL
Allergien
-
Vorherige Impfungen
-

VAERS 1824764

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

gering
Staat
CO
Alter
5,0
Geschlecht
M
Eingang
28.10.2021
Impfdatum
21.10.2021
Beginn
21.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error Wrong product administered

Symptomtext

family came in to receive flu shots but the children received ADACEL instead with no AE; Initial information received on 21-Oct-2021 regarding an unsolicited valid non-serious case received from an other health professional. This case involves a 5-year-old male patient whom it was reported "family came in to receive flu shots [INFLUENZA VACCINE] but the children received DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] instead (wrong product administered)". The patient medical history, medical treatment(s), vaccination(s), concomitant medication and family history were not provided. On 21-Oct-2021, the patient received a 0.5 mL dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [lot U7055BA and expiry date: 03-Jun-2023] via an unknown route in the right arm for prophylactic vaccination. It was a case of actual medication error due to wrong product administered [Latency: on the same day]. At time of reporting, the outcome was unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1824763

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7055BA

gering
Staat
CO
Alter
2,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
21.10.2021
Beginn
21.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Wrong product administered

Symptomtext

a family came in together for flu shots, but the children received ADACEL instead with no AE; Initial information was received on 21-Oct-2021 regarding an unsolicited valid non-serious case received via an other health care professional via a physician via phone (under agency Inquiry Number: 00822801). This case is linked to cluster case US-SA-2021SA353235. This case involves a 24 months old female patient who received DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] instead of INFLUENZA VACCINE with no reported adverse event (wrong product administered). The patient's medical history, past medical treatments, concomitant medications, vaccinations and family history were not provided. On 21-Oct-2021, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot number: U7055BA and expiry date: 30-Jun-2023) via unknown route in the right thigh for prophylactic vaccination. It was a case of an actual medication error due to wrong vaccine administered (Latency: same day). It was reported "Caller states that a family came in together for flu shots, but the children received ADACEL instead of the flu shot. Caller would like to know if there is any safety issue and how will this affect their dosing schedule." At the time of reporting, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-